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| Open AccessWhole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
- Anthony M. Musolf
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| Open AccessNext-generation sequencing of host genetics risk factors associated with COVID-19 severity and long-COVID in Colombian population
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| Open AccessExpression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes
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| Open AccessFully automated landmarking and facial segmentation on 3D photographs
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| Open AccessPatient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey
- Alexis Ceecee Britten-Jones
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| Open AccessCausal relationship between telomere length and sepsis: a bidirectional Mendelian randomization study
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| Open AccessInvestigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss
- Peiliang Lei
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| Open AccessEthnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity
- Lilia Romdhane
- , Sameh Kefi
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| Open AccessLinks between the genetic determinants of morning plasma cortisol and body shape: a two-sample Mendelian randomisation study
- Sofia Christakoudi
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| Open AccessA genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death
- Francesca Minnai
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| Open AccessLinking gene expression to clinical outcomes in pediatric Crohn’s disease using machine learning
- Kevin A. Chen
- , Nina C. Nishiyama
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| Open AccessInteraural and sex differences in the natural evolution of hearing levels in pre-symptomatic and symptomatic carriers of the p.Pro51Ser variant in the COCH gene
- Julie Moyaert
- , Annick Gilles
- & Vincent Van Rompaey
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| Open AccessCombined clinical and ultrasound criteria could accurately predict the Y chromosome in primary amenorrhea patient
- Kanadi Sumapraja
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- & Mila Maidarti
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| Open AccessGamma-glutamyl transferase and calculus of kidney incidence: a Mendelian randomization study
- Peizhe Li
- , Yuewen Pang
- & Jing Shi
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| Open AccessFetuin-A and its genetic association with cardiometabolic disease
- Lawien Al Ali
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- & Pim van der Harst
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| Open AccessNAxtra magnetic nanoparticles for low-cost, efficient isolation of mammalian DNA and RNA
- Eirin Johannessen Starheim
- , Erlend Ravlo
- & Magnar Bjørås
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| Open AccessGenetic sexing of subadult skeletal remains
- Irena Zupanič Pajnič
- , Teo Mlinšek
- & Tamara Leskovar
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| Open AccessUpdate from a cohort study for birth defects in Hunan Province, China, 2010–2020
- Xu Zhou
- , Shenglan Cai
- & Aihua Wang
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| Open AccessAllelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patients
- Dong Woo Nam
- , Yong Keun Song
- & Sang-Yeon Lee
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| Open AccessAssessing causality between osteoarthritis and gastrointestinal disorders: a Mendelian randomization study
- Huiqing Xu
- , Jiahe Wei
- & Qing Shen
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| Open AccessCannabis use and the risk of primary open-angle glaucoma: a Mendelian randomization study
- Andreas Katsimpris
- , Sebastian-Edgar Baumeister
- & Michael Nolde
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| Open AccessHepatic Runx1t1 improves body fat index after endurance exercise in obese mice
- Ning Jiang
- , Zhe Wang
- & Yunlong Cui
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| Open AccessImpact of germline DNA repair gene variants on prognosis and treatment of men with advanced prostate cancer
- Emma B. Hansen
- , Questa Karlsson
- & Karina D. Sørensen
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| Open AccessCYP1A2 expression rather than genotype is associated with olanzapine concentration in psychiatric patients
- Ferenc Fekete
- , Ádám Menus
- & Katalin Monostory
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| Open AccessGenetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection
- Kathleen Ferar
- , Taryn O. Hall
- & David R. Crosslin
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| Open AccessComparative analysis of batch correction methods for FDG PET/CT using metabolic radiogenomic data of lung cancer patients
- Hyunjong Lee
- , Sujin Seo
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| Open AccessNovel GPR156 variants confirm its role in moderate sensorineural hearing loss
- Memoona Ramzan
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| Open AccessChronic inflammation does not mediate the effect of adiposity on grip strength: results from a multivariable Mendelian randomization study
- Tom Norris
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| Open AccessInvestigation of blood group genotype prevalence in Korean population using large genomic databases
- Cheol O Bae
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- & Sinyoung Kim
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| Open AccessSnoring-related polygenic risk and its relationship with lifestyle factors in a Korean population: KoGES study
- Borim Ryu
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| Open AccessGene expression changes in sickle cell reticulocytes and their clinical associations
- Xu Zhang
- , Jihyun Song
- & Victor R. Gordeuk
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| Open AccessAssociation between CYP2B6 genetic variability and cyclophosphamide therapy in pediatric patients with neuroblastoma
- Katalin Mangó
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- & Katalin Monostory
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| Open AccessArteriovenous malformation Map2k1 mutation affects vasculogenesis
- Christopher L. Sudduth
- , Patrick J. Smits
- & Arin K. Greene
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| Open AccessThe effectiveness of optimal exercise-based strategy for patients with hip fracture: a systematic review and Bayesian network meta-analysis
- Rong-jia Pan
- , Si-jie Gui
- & Dan Peng
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| Open AccessDifferential expression of Dusp1 and immediate early response genes in the hippocampus of rats, subjected to forced swim test
- Ivan Vlasov
- , Elena Filatova
- & Maria Shadrina
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| Open AccessDiagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification
- Worakawee Chumworathayee
- , Thongperm Munkongdee
- & Saovaros Svasti
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| Open AccessInteraction of fatty acid quality indices and genes related to lipid homeostasis on mental health among overweight and obese women
- Niloufar Rasaei
- , Alireza Khadem
- & Khadijeh Mirzaei
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| Open AccessSix-year trajectories and associated factors of positive and negative symptoms in schizophrenia patients, siblings, and controls: Genetic Risk and Outcome of Psychosis (GROUP) study
- Tesfa Dejenie Habtewold
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| Open AccessRNA-Seq–based transcriptome analysis of corneal endothelial cells derived from patients with Fuchs endothelial corneal dystrophy
- Tatsuya Nakagawa
- , Yuichi Tokuda
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| Open AccessAPOE ɛ4, but not polygenic Alzheimer’s disease risk, is related to longitudinal decrease in hippocampal brain activity in non-demented individuals
- Sofia Håglin
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| Open AccessGenomic surveillance identifies potential risk factors for SARS-CoV-2 transmission at a mid-sized university in a small rural town
- Kimberly R. Andrews
- , Daniel D. New
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| Open AccessEffect of basal metabolic rate on lifespan: a sex-specific Mendelian randomization study
- Jack C. M. Ng
- & C. Mary Schooling
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| Open AccessIdentification of a genomic DNA sequence that quantitatively modulates KLF1 transcription factor expression in differentiating human hematopoietic cells
- M. N. Gnanapragasam
- , A. Planutis
- & J. J. Bieker
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| Open AccessMutation analysis of pathogenic non-synonymous single nucleotide polymorphisms (nsSNPs) in WFS1 gene through computational approaches
- Jing Zhao
- , Siqi Zhang
- & Qingwen Zhu
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| Open AccessCorrelation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosis
- Naoki Oishi
- , Masaru Noguchi
- & Tatsuo Matsunaga
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| Open AccessGenetic risk of depression is different in subgroups of dietary ratio of tryptophan to large neutral amino acids
- Bence Bruncsics
- , Gabor Hullam
- & Gabriella Juhasz
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| Open AccessArtificial intelligence-based clustering and characterization of Parkinson's disease trajectories
- Colin Birkenbihl
- , Ashar Ahmad
- & Holger Fröhlich
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| Open AccessImpact of gene alterations on clinical outcome in young adults with myelodysplastic syndromes
- Tatsuya Konishi
- , Daichi Sadato
- & Noriko Doki
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| Open AccessGenetic predisposition to smoking in relation to the risk of frailty in ageing
- Wei Liu
- , Hong Yang
- & Yingying Mao